Exela Pharma Sciences
Exela Pharma Sciences
Applications Closed
Posted 4 months ago
Internship
Lenoir, North Carolina
In Person
Smart Summary
The L&D Intern assists in the creation and administration of training programs and initiatives. Responsibilities include scheduling training sessions, preparing documentation, and supporting learners in the Learning Lab.
This internship is for high school students (juniors or seniors preferred) to assist with the creation, administration, and organization of company training programs. Key requirements include excellent English communication skills, critical thinking abilities, proficiency in basic computer programs (Word/PowerPoint/Excel), and the ability to work both independently and as part of a team.
Must Have Skills for ATS
Communication Skills
Critical Thinking
Professional Judgment
Decision-Making Skills
Teamwork
Independence
Computer Skills
Training Development
Event Coordination
Documentation Preparation
Feedback Facilitation
Record Maintenance
Scheduling
Presentation Skills
Learning Support
Administrative Support
Job Description
Position Summary
The L&D Intern helps in the creation, administration, organization and presentation of company trainings, programs, meetings, and initiatives. The primary responsibilities of this role include supporting the creation of learning and development initiatives and programs, assisting with, and scheduling learning opportunities.
*Must be enrolled in High School*
Job Responsibilities
Experience Requirements
Education Requirements
Exela Pharma Sciences
Exela Pharma Sciences, a fast-growing specialty pharmaceutical company, focuses on developing, manufacturing and marketing generic and proprietary injectable and sterile ophthalmic products that keep the healthcare provider and patient in mind. Our goal is to deliver high quality, affordable products that make a difference in people’s lives, and also meet the needs of the healthcare providers that treat them. Exela targets the development and manufacturing of generic and proprietary injectable and sterile ophthalmic products with high barriers to market entry, via an Abbreviated New Drug Approval or 505(b)(2) regulatory pathway. We develop products that enhance the patient or provider experience such as easing the burden of administration, providing an improved safety profile, faster drug preparation, or reduce drug waste. In other words, we strive to improve patient outcomes while reducing overall health care costs.
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